Inga Ebermann

1.5k total citations
19 papers, 1.1k citations indexed

About

Inga Ebermann is a scholar working on Molecular Biology, Sensory Systems and Neurology. According to data from OpenAlex, Inga Ebermann has authored 19 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Sensory Systems and 3 papers in Neurology. Recurrent topics in Inga Ebermann's work include Hearing, Cochlea, Tinnitus, Genetics (12 papers), Retinal Development and Disorders (5 papers) and Connexins and lens biology (4 papers). Inga Ebermann is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (12 papers), Retinal Development and Disorders (5 papers) and Connexins and lens biology (4 papers). Inga Ebermann collaborates with scholars based in Germany, Canada and Lebanon. Inga Ebermann's co-authors include Hanno J. Bolz, Peter Nürnberg, Gudrun Nürnberg, Peter Charbel Issa, Hendrik P. N. Scholl, Robert K. Koenekoop, Claudia Dafinger, Elvir Bećirović, Irma López and José M. Millán and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Cell Biology and Neurology.

In The Last Decade

Inga Ebermann

19 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Inga Ebermann Germany 15 845 433 232 162 144 19 1.1k
Tina Märker Germany 13 1.0k 1.2× 490 1.1× 348 1.5× 160 1.0× 248 1.7× 17 1.3k
Eeva‐Marja Sankila Finland 18 811 1.0× 345 0.8× 198 0.9× 115 0.7× 141 1.0× 38 1.1k
Teresa Jaijo Spain 22 984 1.2× 597 1.4× 151 0.7× 264 1.6× 102 0.7× 58 1.4k
Elena Aller Spain 26 1.8k 2.2× 863 2.0× 243 1.0× 304 1.9× 175 1.2× 55 2.3k
Nanna Dahl Rendtorff Denmark 19 487 0.6× 223 0.5× 136 0.6× 109 0.7× 153 1.1× 40 816
Pavel Seeman Czechia 22 778 0.9× 299 0.7× 289 1.2× 387 2.4× 201 1.4× 99 1.6k
Jacquie Greenberg South Africa 18 927 1.1× 144 0.3× 187 0.8× 62 0.4× 135 0.9× 44 1.3k
Haris Kokotas Greece 14 363 0.4× 197 0.5× 107 0.5× 101 0.6× 29 0.2× 31 637
Shigeyasu Nakai Japan 6 764 0.9× 153 0.4× 156 0.7× 57 0.4× 56 0.4× 7 1.0k
Diana Mitter Germany 15 572 0.7× 121 0.3× 390 1.7× 47 0.3× 152 1.1× 28 923

Countries citing papers authored by Inga Ebermann

Since Specialization
Citations

This map shows the geographic impact of Inga Ebermann's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Inga Ebermann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Inga Ebermann more than expected).

Fields of papers citing papers by Inga Ebermann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Inga Ebermann. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Inga Ebermann. The network helps show where Inga Ebermann may publish in the future.

Co-authorship network of co-authors of Inga Ebermann

This figure shows the co-authorship network connecting the top 25 collaborators of Inga Ebermann. A scholar is included among the top collaborators of Inga Ebermann based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Inga Ebermann. Inga Ebermann is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Thoenes, Michaela, Ulrike Zimmermann, Inga Ebermann, et al.. (2015). OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67). Orphanet Journal of Rare Diseases. 10(1). 15–15. 46 indexed citations
2.
Elsayed, Solaf M., Raoul Heller, Michaela Thoenes, et al.. (2013). Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations. European Journal of Human Genetics. 22(2). 286–288. 28 indexed citations
3.
Eisenberger, Tobias, Rima Slim, Ahmad M. Mansour, et al.. (2012). Targeted next-generation sequencing identifies a homozygous nonsense mutation in ABHD12, the gene underlying PHARC, in a family clinically diagnosed with Usher syndrome type 3. Orphanet Journal of Rare Diseases. 7(1). 59–59. 60 indexed citations
4.
Sahly, Iman, Éric Dufour, Cataldo Schietroma, et al.. (2012). Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice. The Journal of Cell Biology. 199(2). 381–399. 127 indexed citations
5.
Dafinger, Claudia, Max C. Liebau, Solaf M. Elsayed, et al.. (2011). Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics. Journal of Clinical Investigation. 121(7). 2662–2667. 141 indexed citations
6.
Ebermann, Inga, Jennifer B. Phillips, Max C. Liebau, et al.. (2011). PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome. Journal of Clinical Investigation. 121(2). 821–821. 9 indexed citations
7.
Aller, Elena, Teresa Jaijo, Erwin van Wijk, et al.. (2010). Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse origin.. PubMed. 16. 495–500. 14 indexed citations
8.
Ebermann, Inga, Jennifer B. Phillips, Max C. Liebau, et al.. (2010). PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome. Journal of Clinical Investigation. 120(6). 1812–1823. 181 indexed citations
9.
Issa, Peter Charbel, et al.. (2009). Characterisation of severe rod-cone dystrophy in a consanguineous family with a splice site mutation in the MERTK gene. British Journal of Ophthalmology. 93(7). 920–925. 51 indexed citations
10.
Ebermann, Inga, Martin H. J. Wiesen, Eberhart Zrenner, et al.. (2009). GPR98 mutations cause Usher syndrome type 2 in males. Journal of Medical Genetics. 46(4). 277–280. 28 indexed citations
11.
Mégarbané, André, Rima Slim, Gudrun Nürnberg, et al.. (2009). A novel VPS13B mutation in two brothers with Cohen syndrome, cutis verticis gyrata and sensorineural deafness. European Journal of Human Genetics. 17(8). 1076–1079. 10 indexed citations
12.
Ebermann, Inga, et al.. (2008). An USH2A founder mutation is the major cause of Usher syndrome type 2 in Canadians of French origin and confirms common roots of Quebecois and Acadians. European Journal of Human Genetics. 17(1). 80–84. 28 indexed citations
13.
Bećirović, Elvir, et al.. (2008). Usher syndrome type 1 due to missense mutations on bothCDH23 alleles: investigation of mRNA splicing. Human Mutation. 29(3). 452–452. 29 indexed citations
14.
Ebermann, Inga, Solaf M. Elsayed, Gudrun Nürnberg, et al.. (2008). DOUBLE HOMOZYGOSITY FOR MUTATIONS OF AGL AND SCN9A MIMICKING NEUROHEPATOPATHY SYNDROME. Neurology. 70(24). 2343–2344. 7 indexed citations
15.
Ebermann, Inga, Martin Walger, Hendrik P. N. Scholl, et al.. (2007). Truncating mutation of theDFNB59gene causes cochlear hearing impairment and central vestibular dysfunction. Human Mutation. 28(6). 571–577. 73 indexed citations
16.
Ebermann, Inga, Irma López, Maria Bitner‐Glindzicz, et al.. (2007). Deafblindness in French Canadians from Quebec: a predominant founder mutation in the USH1Cgene provides the first genetic link with the Acadian population. Genome biology. 8(4). R47–R47. 36 indexed citations
17.
Ebermann, Inga, et al.. (2007). Two truncating USH3A mutations, including one novel, in a German family with Usher syndrome.. PubMed. 13. 1539–47. 12 indexed citations
18.
Ebermann, Inga, Hendrik P. N. Scholl, Peter Charbel Issa, et al.. (2006). A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss. Human Genetics. 121(2). 203–211. 173 indexed citations
19.
Bolz, Hanno J., Inga Ebermann, & Andreas Gal. (2005). Protocadherin-21 (PCDH21), a candidate gene for human retinal dystrophies.. PubMed. 11. 929–33. 18 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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